STX2 is a causative gene for nonobstructive azoospermia

Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations

(2017) S. Nakamura et al.   Andrology

Single gene defects leading to sperm quantitative anomalies

(2016) M.J. Mitchell et al.   CLINICAL GENETICS

Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia

(2015) Esther Maor-Sagie et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

(2015) Alexander N. Yatsenko et al.   NEW ENGLAND JOURNAL OF MEDICINE

Truncating mutations inTAF4BandZMYND15causing recessive azoospermia

(2014) Özgecan Ayhan et al.   JOURNAL OF MEDICAL GENETICS

t-SNARE Syntaxin2 (STX2) Is Implicated in Intracellular Transport of Sulfoglycolipids During Meiotic Prophase in Mouse Spermatogenesis

(2013) Y. Fujiwara et al.   BIOLOGY OF REPRODUCTION

Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships

(2012) Kristen Lipscomb Sund et al.   GENETICS IN MEDICINE

Multinucleated spermatocytes in the aging human testis: formation, morphology, and degenerative fate

(2010) A. Miething   ANDROLOGIA

A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest

(2009) Toshinobu Miyamoto et al.   ASIAN JOURNAL OF ANDROLOGY